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人类和小鼠MOG基因在MHC Ib类区域远端的物理图谱。

Physical mapping of the human and mouse MOG gene at the distal end of the MHC class Ib region.

作者信息

Pham-Dinh D, Jones E P, Pitiot G, Della Gaspera B, Daubas P, Mallet J, Le Paslier D, Fischer Lindahl K, Dautigny A

机构信息

Laboratoire de Neurogénétique Moléculaire, Centre National de la Recherche Scientifique, Unité 1488, Institut des Neurosciences, Université de Paris VI, 9 quai Saint Bernard, F-75252 Paris Cedex 05, France.

出版信息

Immunogenetics. 1995;42(5):386-91. doi: 10.1007/BF00179400.

Abstract

Myelin/oligodendrocyte glycoprotein (MOG) is expressed specifically in the central nervous system (CNS) by myelinating glial cells, the oligodendrocytes. The external location of MOG on myelin sheaths and its late expression during myelinogenesis argue for a role of MOG in the completion of myelin and maintenance of its integrity. MOG is a target autoantigen in demyelinating diseases, such as experimental autoimmune encephalomyelitis (EAE) in animals and multiple sclerosis (MS) in humans. We previously located the gene encoding MOG to the major histocompatibility complex (MHC), both in human, by cytogenetics, and in mouse, by analysis of recombinants. To refine the position, we have now selected yeast artificial chromosome clones (YAC) which contain the MOG gene. Physical mapping of the human MOG and the mouse Mog genes by characterization of these YAC clones indicated that the gene is located at the distal end of the major histocompatibility complex (MHC) class Ib region in both species. The human MOG gene lies 60 kilobases (kb) telomeric to HLA-F in a head-to-head orientation; the mouse Mog gene lies 25 (kb) telomeric to H2-M5 in a tail-to-head orientation. These orthologous genes provide markers for comparative analysis of the evolution of the MHC in the two species. The physical mapping of MOG should facilitate analysis of its role in hereditary neurological diseases, and the YAC clones identified here will permit the identification of new genes in the region.

摘要

髓鞘/少突胶质细胞糖蛋白(MOG)由髓鞘形成性神经胶质细胞即少突胶质细胞在中枢神经系统(CNS)中特异性表达。MOG在髓鞘膜上的外部位置及其在髓鞘形成过程中的晚期表达表明,MOG在髓鞘的完成及其完整性的维持中发挥作用。MOG是脱髓鞘疾病中的一种靶自身抗原,如动物实验性自身免疫性脑脊髓炎(EAE)和人类多发性硬化症(MS)。我们之前通过细胞遗传学将编码MOG的基因定位到人类的主要组织相容性复合体(MHC),并通过重组分析将其定位到小鼠的MHC。为了精确该位置,我们现在选择了包含MOG基因的酵母人工染色体克隆(YAC)。通过对这些YAC克隆的特征分析对人类MOG基因和小鼠Mog基因进行物理图谱绘制,结果表明该基因在两个物种中均位于主要组织相容性复合体(MHC)Ib类区域的远端。人类MOG基因以头对头的方向位于HLA - F端粒60千碱基(kb)处;小鼠Mog基因以尾对头的方向位于H2 - M5端粒25(kb)处。这些直系同源基因提供了用于比较分析两个物种中MHC进化的标记。MOG的物理图谱绘制应有助于分析其在遗传性神经疾病中的作用,此处鉴定的YAC克隆将有助于鉴定该区域的新基因。

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